Inhibition of tumor necrosis factor-induced apoptosis in transgenic mouse liver expressing creatine kinase

Liver Int. 2004 Aug;24(4):384-93. doi: 10.1111/j.1478-3231.2004.0939.x.

Abstract

Background: The mitochondrion acts as a pivotal decision center in many types of apoptotic responses. To clarify the effects of the enhanced mitochondrial function on tumor necrosis factoralpha (TNFalpha)-induced apoptosis, we studied hepatic injuries in transgenic mice whose livers express creatine kinase (CK).

Methods: Mice fed a diet containing 10% creatine, came to accumulate phosphocreatine and to enhance hepatic ATP levels and mitochondrial oxidative phosphorylation activities. TNFalpha-mediated hepatic apoptosis in normally fed and Cr-feeding CK transgenic mice were assessed.

Results: TNFalpha and actinomycin D cause severe liver failure in normally fed transgenic mice, and in the wild-type mice. In contrast, no significant elevations in transaminase levels after injection were observed in Cr feeding transgenic mice. The disruption of the mitochondrial transmembrane potential at 2 h after TNFalpha injection, prior to ATP depletion, activation of caspase 3 like protease, and DNA fragmentation at 4-6 h after injection, were observed in normally fed transgenic mice. These were fully suppressed in Cr feeding transgenic mice. However, anti-Fas antibody-induced apoptosis was not inhibited in both groups.

Conclusions: The results indicate that TNFalpha-induced apoptosis was inhibited in CK transgenic mice livers by maintaining mitochondrial function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / metabolism
  • Adenosine Diphosphate / metabolism
  • Adenosine Triphosphate / metabolism
  • Animals
  • Caspase 3
  • Caspases / metabolism
  • Creatine Kinase / genetics*
  • DNA Fragmentation / physiology*
  • Liver / enzymology*
  • Liver / pathology
  • Liver Failure / metabolism*
  • Liver Failure / pathology
  • Liver Failure / physiopathology
  • Membrane Potentials
  • Mice
  • Mice, Transgenic
  • Mitochondria / physiology
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Tumor Necrosis Factor-alpha
  • Adenosine Diphosphate
  • Adenosine Triphosphate
  • Creatine Kinase
  • Casp3 protein, mouse
  • Caspase 3
  • Caspases
  • Adenine